Managing idiopathic short stature: role of somatropin (rDNA origin) for injection

J Paul Frindik1, Stephen F Kemp11University of Arkansas for Medical Sciences and Arkansas Children’s Hospital, AR, USAAbstract: Idiopathic short stature (ISS) is a term that describes short stature in children who do not have growth hormone (GH) deficiency and in whom the etiology of t...

Descripción completa

Guardado en:
Detalles Bibliográficos
Autores principales: J Paul Frindik, Stephen F Kemp
Formato: article
Lenguaje:EN
Publicado: Dove Medical Press 2010
Materias:
Acceso en línea:https://doaj.org/article/235c49d9bd574a9f828f85a8bfcec195
Etiquetas: Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
id oai:doaj.org-article:235c49d9bd574a9f828f85a8bfcec195
record_format dspace
spelling oai:doaj.org-article:235c49d9bd574a9f828f85a8bfcec1952021-12-02T02:02:36ZManaging idiopathic short stature: role of somatropin (rDNA origin) for injection1177-54751177-5491https://doaj.org/article/235c49d9bd574a9f828f85a8bfcec1952010-06-01T00:00:00Zhttp://www.dovepress.com/managing-idiopathic-short-stature-role-of-somatropin-rdna-origin-for-i-a4563https://doaj.org/toc/1177-5475https://doaj.org/toc/1177-5491J Paul Frindik1, Stephen F Kemp11University of Arkansas for Medical Sciences and Arkansas Children’s Hospital, AR, USAAbstract: Idiopathic short stature (ISS) is a term that describes short stature in children who do not have growth hormone (GH) deficiency and in whom the etiology of the short stature is not identified. Between 1985 and 2000, more than 40 studies were published regarding GH therapy for ISS. Only 12 of these had data to adult height, of which only 4 were controlled studies. A subsequent placebo-controlled study that followed subjects to adult height indicated that there was a gain of 3.7–7.5 cm in height with GH treatment. In 2003, the US Federal Drug Administration (FDA) approved GH for treatment of short stature. Even before FDA approval, patients with ISS made up about 20% of patients in GH databases, which is largely unchanged since FDA approval. There remains some controversy as to whether GH should be used to treat ISS. This controversy centers on the fact that there has been no definitive demonstration that short stature results in a disadvantage or problems with psychological adjustment, and thus, no demonstration that GH therapy results in improvement in quality of life.Keywords: idiopathic short stature, ISS, growth hormone therapy, somatotropin, somatropin, insulin-like growth factor I, IGF-1 J Paul FrindikStephen F KempDove Medical PressarticleMedicine (General)R5-920ENBiologics: Targets & Therapy, Vol 2010, Iss default, Pp 147-155 (2010)
institution DOAJ
collection DOAJ
language EN
topic Medicine (General)
R5-920
spellingShingle Medicine (General)
R5-920
J Paul Frindik
Stephen F Kemp
Managing idiopathic short stature: role of somatropin (rDNA origin) for injection
description J Paul Frindik1, Stephen F Kemp11University of Arkansas for Medical Sciences and Arkansas Children’s Hospital, AR, USAAbstract: Idiopathic short stature (ISS) is a term that describes short stature in children who do not have growth hormone (GH) deficiency and in whom the etiology of the short stature is not identified. Between 1985 and 2000, more than 40 studies were published regarding GH therapy for ISS. Only 12 of these had data to adult height, of which only 4 were controlled studies. A subsequent placebo-controlled study that followed subjects to adult height indicated that there was a gain of 3.7–7.5 cm in height with GH treatment. In 2003, the US Federal Drug Administration (FDA) approved GH for treatment of short stature. Even before FDA approval, patients with ISS made up about 20% of patients in GH databases, which is largely unchanged since FDA approval. There remains some controversy as to whether GH should be used to treat ISS. This controversy centers on the fact that there has been no definitive demonstration that short stature results in a disadvantage or problems with psychological adjustment, and thus, no demonstration that GH therapy results in improvement in quality of life.Keywords: idiopathic short stature, ISS, growth hormone therapy, somatotropin, somatropin, insulin-like growth factor I, IGF-1
format article
author J Paul Frindik
Stephen F Kemp
author_facet J Paul Frindik
Stephen F Kemp
author_sort J Paul Frindik
title Managing idiopathic short stature: role of somatropin (rDNA origin) for injection
title_short Managing idiopathic short stature: role of somatropin (rDNA origin) for injection
title_full Managing idiopathic short stature: role of somatropin (rDNA origin) for injection
title_fullStr Managing idiopathic short stature: role of somatropin (rDNA origin) for injection
title_full_unstemmed Managing idiopathic short stature: role of somatropin (rDNA origin) for injection
title_sort managing idiopathic short stature: role of somatropin (rdna origin) for injection
publisher Dove Medical Press
publishDate 2010
url https://doaj.org/article/235c49d9bd574a9f828f85a8bfcec195
work_keys_str_mv AT jpaulfrindik managingidiopathicshortstatureroleofsomatropinrdnaoriginforinjection
AT stephenfkemp managingidiopathicshortstatureroleofsomatropinrdnaoriginforinjection
_version_ 1718402697544073216